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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419224Generated: November 2, 2026

Dicyclohexylcarbodiimide → HCID 178512532, compound

https://huagongshe.com/reaction/1419224

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantMethanesulfonateHCID 85257—
Reactant6-Amidino-1-carbamoylmethyl-2-naphthol.hydrochlorideHCID 136454270—
ReactantHCID 178512548HCID 178512548—
SolventMethanolHCID 887—
SolventPyridineHCID 1049—
ProductHCID 178512532HCID 17851253266.9%

Reaction Steps

100 Milliliters of 20% hydrous pyridine was added to 3.0 g of 4-guanidinobenzoic acid.methanesulfonate, 3.0 g of 6-amidino-1-carbamoylmethyl-2-naphthol.hydrochloride and 4.5 g of DCC, followed by stirring for 2 hours under cooling with ice and then 2 days at room temperature. The precipitate was filtered and 1 g of active carbon was added to the filtrate, followed by stirring for 30 minutes under cooling with ice, and insoluble matter was filtered off. The filtrate was slowly added dropwise to 4 liters of ether under cooling with ice, followed by stirring for 2 hours. The precipitate was collected by filtration and washed with 100 ml of acetone to obtain a crude product. Then, the product was dissolved in 150 ml of methanol. Thereafter, 2.5 g of active carbon was added to the solution, followed by stirring for 30 minutes under cooling with ice, and insoluble matter was filtered off. The filtrate was slowly added dropwise to 1 liter of acetone under cooling with ice, followed by stirring for 2 hours. The precipitate was collected by filtration to obtain 2.9 g of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05885990
Source datasetuspto-grants-1999_03
ORD IDord-698169006f1644d9ac9f68003bcfa197
Source noteuspto-grants-1999_03